A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599440



Internal ID6986487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3904368..3991525hg38UCSC Ensembl
chr4:3906095..3993252hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3887158
hg1987158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11317814, essv11317816, essv11317812, essv11317810, essv11317811, essv11317818, essv11317815, essv11317817, essv11317813, essv11317809
SamplesHG03559, HG02891, HG02485, HG01444, NA19473, HG03157, HG03896, NA20528, HG03303, HG03265
Known GenesFAM86EP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599440
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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